US2230624A - Extraction of protein from peanuts - Google Patents
Extraction of protein from peanuts Download PDFInfo
- Publication number
- US2230624A US2230624A US254741A US25474139A US2230624A US 2230624 A US2230624 A US 2230624A US 254741 A US254741 A US 254741A US 25474139 A US25474139 A US 25474139A US 2230624 A US2230624 A US 2230624A
- Authority
- US
- United States
- Prior art keywords
- protein
- solution
- peanuts
- alkaline
- extraction
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 108090000623 proteins and genes Proteins 0.000 title description 20
- 102000004169 proteins and genes Human genes 0.000 title description 20
- 235000020232 peanut Nutrition 0.000 title description 16
- 238000000605 extraction Methods 0.000 title description 11
- 241001553178 Arachis glabrata Species 0.000 title 1
- 239000000243 solution Substances 0.000 description 22
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- 244000105624 Arachis hypogaea Species 0.000 description 15
- 238000000034 method Methods 0.000 description 13
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 102000006395 Globulins Human genes 0.000 description 7
- 108010044091 Globulins Proteins 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 6
- 239000004202 carbamide Substances 0.000 description 6
- 235000014571 nuts Nutrition 0.000 description 6
- 235000011121 sodium hydroxide Nutrition 0.000 description 6
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 6
- 235000017060 Arachis glabrata Nutrition 0.000 description 5
- 235000010777 Arachis hypogaea Nutrition 0.000 description 5
- 235000018262 Arachis monticola Nutrition 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 5
- 235000010269 sulphur dioxide Nutrition 0.000 description 5
- 239000004291 sulphur dioxide Substances 0.000 description 5
- 238000007792 addition Methods 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 239000012670 alkaline solution Substances 0.000 description 4
- 235000012054 meals Nutrition 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000009987 spinning Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 3
- 239000000284 extract Substances 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- BELBBZDIHDAJOR-UHFFFAOYSA-N Phenolsulfonephthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2S(=O)(=O)O1 BELBBZDIHDAJOR-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- OBRMNDMBJQTZHV-UHFFFAOYSA-N cresol red Chemical compound C1=C(O)C(C)=CC(C2(C3=CC=CC=C3S(=O)(=O)O2)C=2C=C(C)C(O)=CC=2)=C1 OBRMNDMBJQTZHV-UHFFFAOYSA-N 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000020477 pH reduction Effects 0.000 description 2
- 229960003531 phenolsulfonphthalein Drugs 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- RTZZCYNQPHTPPL-UHFFFAOYSA-N 3-nitrophenol Chemical compound OC1=CC=CC([N+]([O-])=O)=C1 RTZZCYNQPHTPPL-UHFFFAOYSA-N 0.000 description 1
- 108010002493 Arachin Proteins 0.000 description 1
- 241000220438 Arachis Species 0.000 description 1
- 235000003911 Arachis Nutrition 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 206010033546 Pallor Diseases 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- UDSAIICHUKSCKT-UHFFFAOYSA-N bromophenol blue Chemical compound C1=C(Br)C(O)=C(Br)C=C1C1(C=2C=C(Br)C(O)=C(Br)C=2)C2=CC=CC=C2S(=O)(=O)O1 UDSAIICHUKSCKT-UHFFFAOYSA-N 0.000 description 1
- NUHCTOLBWMJMLX-UHFFFAOYSA-N bromothymol blue Chemical compound BrC1=C(O)C(C(C)C)=CC(C2(C3=CC=CC=C3S(=O)(=O)O2)C=2C(=C(Br)C(O)=C(C(C)C)C=2)C)=C1C NUHCTOLBWMJMLX-UHFFFAOYSA-N 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- WNPXRNJEBMRJGV-UHFFFAOYSA-N chembl1399590 Chemical compound COC1=CC=CC(C=2N=C3C=CC=CC3=C(N3C(CCCC3)C)N=2)=C1O WNPXRNJEBMRJGV-UHFFFAOYSA-N 0.000 description 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 239000003398 denaturant Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- STZCRXQWRGQSJD-GEEYTBSJSA-M methyl orange Chemical compound [Na+].C1=CC(N(C)C)=CC=C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 STZCRXQWRGQSJD-GEEYTBSJSA-M 0.000 description 1
- 229940012189 methyl orange Drugs 0.000 description 1
- PGSADBUBUOPOJS-UHFFFAOYSA-N neutral red Chemical compound Cl.C1=C(C)C(N)=CC2=NC3=CC(N(C)C)=CC=C3N=C21 PGSADBUBUOPOJS-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- PRZSXZWFJHEZBJ-UHFFFAOYSA-N thymol blue Chemical compound C1=C(O)C(C(C)C)=CC(C2(C3=CC=CC=C3S(=O)(=O)O2)C=2C(=CC(O)=C(C(C)C)C=2)C)=C1C PRZSXZWFJHEZBJ-UHFFFAOYSA-N 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000002166 wet spinning Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
- A23J1/00—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites
- A23J1/14—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites from leguminous or other vegetable seeds; from press-cake or oil-bearing seeds
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F4/00—Monocomponent artificial filaments or the like of proteins; Manufacture thereof
Definitions
- This invention relates to the extraction of proteins from peanuts; and it comprises a method of extracting the globulins in colorless form from residues left in regaining oil from peanuts wherein the residues are extracted with an alkaline aqueous solution at a pH not exceeding 8.5 at anytime and being 8 to 8.5'in the final stages of the extraction, and recovering the globulins from the solution so formed by acidification,
- the globulins (arachin and conarachin) contained in peanuts (Arachis) have been found ,--*to be an advantageous material for the production of artificial fibers, much like wool in their properties and susceptible of being dyed, spun, woven, etc., in much the same manner as wool. In these methods a light-colored material of reasonable purity is desirable. A light color is particularly necessary.
- protein from peanuts is dissolved or dispersed in urea solutions. The urea acts as a denaturant, changing the physical form of the globulin molecule of the protein into one better adapted for mak ing filaments.
- the protein gives a thin dispersion which can be clarified to free it of mechanical impurities and gradually thickens on ageing into a form suitable for extrusion.
- the aged solution is extruded in the ordinary Ways used in making filaments; extrusion being into an aqueous bath adapted to remove the urea. There may or may not be some acid in this bath and the filaments may afterwards he treated in 5 various ways not here important.
- the urea acts as a solvent or peptizing agent. The solvent action may be accelerated by small amounts of othermaterials not here important.
- the object achieved in the present invention is the production of a high yield of light colored
- protein from peanut residues left after extracting oil either residues from blanched or from unblanched nuts.
- the protein removed in the present invention is particularly applicable for fiber-making operations.
- Suitable alkaline materials for use according to my invention are mild or caustic alkalis, such as sodium hydroxide or carbonate, or ammonia, l5 and strongly alkaline salts such as sodium sulfide; alkaline substances strong enough to enable maintenance of the specified pH during the extraction.
- a mixture of indicators such as one of th so-called universal indicators, may be used to follow the change in alkalinity of the solution, or I may use an indicator such as Phenol Red 45 or Cresol Red to show the final stage of the extraction, in conjunction with a more acid indicator such as litmus or Bromthymol Blue (yellow to blue, 6.0-7.6) which gives warning when the acidic material in the nut meal is approach- 50 ing exhaustion.
- the mixture When the mixture has been maintained at the desired alkalinity for a time suflicient for substantially complete extraction of the protein soluble at that alkalinity, the mixture may be setof protein forms.
- the insoluble matter may be stirred up with water and again centrifuged, and the washings added to the main solution; which may then be clarified in e. g. a super-centrifuge of the high-speed type.
- the soluble protein may then be reprecipitated from the solution by a suitable change in the alkalinity; for instance by neutralizing the alkali with sulphur dioxide, or by allowing acid-forming fermentation to occur in the solution.
- the progress of the neutralization may be followed by means of a suitable external indicator; for instance, Methyl Orange (red to yellow, 3.0-4.4) or Bromphenol Blue (yellow to blue 3.0-4.7).
- a suitable external indicator for instance, Methyl Orange (red to yellow, 3.0-4.4) or Bromphenol Blue (yellow to blue 3.0-4.7).
- Example 1 200 parts of extracted peanut meal from unblanched nuts are stirred vigorously with 3500 parts water at 20 C. for 5 to minutes. 330 parts of a 1.2 per cent solution of sodium sul phide are run in over a period of 14 minutes. During the addition hydrogen sulphide is evolved, and the mixture does not appreciably affect the color of red litmus. The bath is not alkaline to litmus. Further addition of the sodium sulphide solution, however, causes a marked rise in the pH value, and the rate of addition of alkali is therefore reduced. At the end of 30 minutes 170 parts of sodium sulphide solution have been added, and the pH value of the solution is found to be approximately 8.0 to 8.5.
- Example 2 200 parts extracted peanut meal from unblanched nuts are stirred vigorously with 3500 parts water at 20 C. as in Example 1.
- 150 parts of a 1.2 per cent solution of sodium hydroxide in water are added over a period of 20 minutes while the mixture is kept stirred.
- the pH value reaches a value of about 8.0-8.5 at the end of the operation. Stirring is continued for one hour.
- After clarification the solution has a pH value of 8.3, and the solution is almost entirely devoid of undesirable color.
- Sulphur dioxide is passed through the solution until the pH value is 4.5, also in the iso-electric region; and the white precipitate of protein is worked up as in Example 1.
- the dry product amounts to 84 parts by weight and is white in color, yielding almost colorless solution in concentrated aqueous urea, which on standing becomes unusually viscous before it gelates. This is an advantageous property.
- the solution may be spun into filaments or excellent color and quality.
- Example 1 instead of the sodium sulphide used in Example 1, I could have used sodium hydroxide, sodium polysulphide, sodium carbonate, sodium cyanide, or the hydroxides or salts of the alkalis and alkaline earths. The point is maintenance of the specified pH range during the extraction rather than the use of any particular alkaline substance. Any salt chosen should of coursebe one without ill effect on the protein.
- This invention is a valuable advance in the art as it enables the protein to be extracted from peanuts by a simple process which omits the expensive blanching step.
- the resulting protein has better spinning qualities than those produced by old methods and will form spinning solutions from which filaments of excellent appearance and physical properties may be obtained by a wet spinning process.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Textile Engineering (AREA)
- Peptides Or Proteins (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4882/38A GB513896A (en) | 1938-02-16 | 1938-02-16 | Improvements in or relating to the extraction of protein from ground nuts |
Publications (1)
Publication Number | Publication Date |
---|---|
US2230624A true US2230624A (en) | 1941-02-04 |
Family
ID=9785608
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US254741A Expired - Lifetime US2230624A (en) | 1938-02-16 | 1939-02-04 | Extraction of protein from peanuts |
Country Status (5)
Country | Link |
---|---|
US (1) | US2230624A (en(2012)) |
DE (1) | DE898946C (en(2012)) |
FR (1) | FR850388A (en(2012)) |
GB (1) | GB513896A (en(2012)) |
NL (1) | NL52770C (en(2012)) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2417576A (en) * | 1943-04-12 | 1947-03-18 | Ici Ltd | Manufacture of viscous protein solutions for the production of artificial filaments |
US2431993A (en) * | 1947-12-02 | Alkali-treating vegetable protein | ||
US2603630A (en) * | 1948-12-31 | 1952-07-15 | Robert S Aries | Method for extracting proteins from yeast |
US2628022A (en) * | 1953-02-10 | Method fob recovering protein from | ||
US2684960A (en) * | 1954-07-27 | Method of isolating protein from |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE417950A (en(2012)) * | 1935-10-22 |
-
0
- NL NL52770D patent/NL52770C/xx active
-
1938
- 1938-02-16 GB GB4882/38A patent/GB513896A/en not_active Expired
-
1939
- 1939-02-04 US US254741A patent/US2230624A/en not_active Expired - Lifetime
- 1939-02-15 DE DEI3040D patent/DE898946C/de not_active Expired
- 1939-02-16 FR FR850388D patent/FR850388A/fr not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2431993A (en) * | 1947-12-02 | Alkali-treating vegetable protein | ||
US2628022A (en) * | 1953-02-10 | Method fob recovering protein from | ||
US2684960A (en) * | 1954-07-27 | Method of isolating protein from | ||
US2417576A (en) * | 1943-04-12 | 1947-03-18 | Ici Ltd | Manufacture of viscous protein solutions for the production of artificial filaments |
US2603630A (en) * | 1948-12-31 | 1952-07-15 | Robert S Aries | Method for extracting proteins from yeast |
Also Published As
Publication number | Publication date |
---|---|
GB513896A (en) | 1939-10-25 |
FR850388A (fr) | 1939-12-15 |
NL52770C (en(2012)) | |
DE898946C (de) | 1953-12-07 |
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